SUNSCREEN MOISTURIZER

Manufacturer
Guangzhou Yanxi Biotechnology Co., Ltd
Effective date
2024-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:08:07

Label at a glance#

ProductSUNSCREEN MOISTURIZER
Active ingredientZINC OXIDE
Label structure3 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only.keep out of reach of children.Avoid contact with eyes.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

INDICATIONS & USAGE SECTION

Many different skin types.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84025-135-01SUNSCREEN MOISTURIZER60 mL in 1 TUBECREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84025-135SUNSCREEN MOISTURIZER (ZINC OXIDE) CREAM [GUANGZHOU YANXI BIOTECHNOLOGY CO., LTD]11 package rows20240201_0fc1b4a2-6f99-0cd2-e063-6394a90ada73.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84025-13584025-135-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0fc1b4a2-6f9a-0cd2-e063-6394a90ada730fc1b4a2-6f99-0cd2-e063-6394a90ada732024-01-25WarningsExact identifier
spl id: 0fc1b4a2-6f9a-0cd2-e063-6394a90ada73
spl set id: 0fc1b4a2-6f99-0cd2-e063-6394a90ada73

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.